Tandem rearrangements of a cyclic bis-allene

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Tandem rearrangements of a cyclic bis-allene. / Mustafa, H.H.; Baird, M.S.; Al-Dulayymi, J.R. et al.
In: Tetrahedron, Vol. 70, No. 7, 18.02.2014, p. 1502-1507.

Research output: Contribution to journalArticlepeer-review

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Mustafa, HH, Baird, MS, Al-Dulayymi, JR & Tverezovskiy, V 2014, 'Tandem rearrangements of a cyclic bis-allene', Tetrahedron, vol. 70, no. 7, pp. 1502-1507. https://doi.org/10.1016/j.tet.2013.12.058

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MLA

Mustafa, H.H. et al. "Tandem rearrangements of a cyclic bis-allene". Tetrahedron. 2014, 70(7). 1502-1507. https://doi.org/10.1016/j.tet.2013.12.058

VancouverVancouver

Mustafa HH, Baird MS, Al-Dulayymi JR, Tverezovskiy V. Tandem rearrangements of a cyclic bis-allene. Tetrahedron. 2014 Feb 18;70(7):1502-1507. Epub 2014 Jan 8. doi: 10.1016/j.tet.2013.12.058

Author

Mustafa, H.H. ; Baird, M.S. ; Al-Dulayymi, J.R. et al. / Tandem rearrangements of a cyclic bis-allene. In: Tetrahedron. 2014 ; Vol. 70, No. 7. pp. 1502-1507.

RIS

TY - JOUR

T1 - Tandem rearrangements of a cyclic bis-allene

AU - Mustafa, H.H.

AU - Baird, M.S.

AU - Al-Dulayymi, J.R.

AU - Tverezovskiy, V.

PY - 2014/2/18

Y1 - 2014/2/18

N2 - Reaction of the bis-dibromocarbene adduct of cyclonona-1,4,7-triene with methyllithium leads to a mixture of meso and racemic cycloundeca-1,2,5,6,9-pentaenes; the former rearranges at ambient temperature through a set of pericyclic reactions

AB - Reaction of the bis-dibromocarbene adduct of cyclonona-1,4,7-triene with methyllithium leads to a mixture of meso and racemic cycloundeca-1,2,5,6,9-pentaenes; the former rearranges at ambient temperature through a set of pericyclic reactions

U2 - 10.1016/j.tet.2013.12.058

DO - 10.1016/j.tet.2013.12.058

M3 - Article

VL - 70

SP - 1502

EP - 1507

JO - Tetrahedron

JF - Tetrahedron

SN - 0040-4020

IS - 7

ER -